ZDHHC21-PHGDH Fusion FISH Probe
The ZDHHC21-PHGDH Fusion FISH Probe is used to confirm a fusion of the ZDHHC21 and PHGDH genes. The fusion of the ZDHHC21 and PHGDH genes has been associated with Skin Cutaneous Melanoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ZDHHC21-PHGDH-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-RERE | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-REOR | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-REGO | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-REGR | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-REAQ | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-ORRE | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-OROR | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-ORGO | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-ORAQ | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GORE | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GOOR | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GOGO | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GOGR | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GOAQ | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GRRE | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GROR | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GRGO | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GRGR | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-GRAQ | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-AQRE | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-AQOR | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-AQGO | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-AQGR | 20 (40 μL) | 200 μL |
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| ZDHHC21-PHGDH-20-AQAQ | 20 (40 μL) | 200 μL |
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PHGDH Gene Summary
This gene encodes the enzyme which is involved in the early steps of L-serine synthesis in animal cells. L-serine is required for D-serine and other amino acid synthesis. The enzyme requires NAD/NADH as a cofactor and forms homotetramers for activity. Mutations in this gene have been found in a family with congenital microcephaly, psychomotor retardation and other symptoms. Multiple alternatively spliced transcript variants have been found, however the full-length nature of most are not known. [provided by RefSeq, Aug 2011]
Gene Name: Phosphoglycerate Dehydrogenase
Chromosome: CHR1: 120254418 -120286849
Locus: 1p12
ZDHHC21 Gene Summary
The Zinc Finger DHHC-type Containing 21 (ZDHHC21) gene is located on chr9 :14611068-14693480 at 9p22.3.
Gene Name: Zinc Finger DHHC-type Containing 21
Chromosome: CHR9: 14611068 -14693480
Locus: 9p22.3
Gene Diseases
The ZDHHC21 PHGDH Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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